Evidence map›Paper›PMID 20681320›Full record

ReviewScience progress2010

Development and regeneration of projection neuron subtypes of the cerebral cortex.

Giulio Srubek Tomassy, Simona Lodato, Zachary Trayes-Gibson, Paola Arlotta

Abstract readReview
In one paragraph

Review in Science progress, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Production and organization of neocortical interneurons.Frontiers in cellular neuroscience · 2013
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Giulio Srubek TomassyMassachusetts General Hospital, Boston, USA. SrubekTomassy.Giulio@mgh.harvard.edu
Simona Lodato
Zachary Trayes-Gibson
Paola Arlotta

Funding

Fate specification of corticospinal neurons by cell autonomous signalingR01NS062849 · NINDS · MASSACHUSETTS GENERAL HOSPITAL · PI ARLOTTA, PAOLA · 2009 to 2013
$1.8M
NINDS NIH HHS NS062849NINDS NIH HHS R01 NS062849
6 · The paper itself

Abstract

The idea of repairing damaged neuronal circuitry in the mammalian central nervous system (CNS) has challenged neuroscientists for centuries. This is mainly due to the notorious inability of neurons to regenerate and the unparalleled cellular diversity of the nervous system. In the mammalian cerebral cortex, one of the most complex areas of the CNS, multipotent neural stem and progenitor cells undergo progressive specification during development to generate the staggering variety of projection neuron subtypes that are found in the adult. How is this process orchestrated in the embryo? And, can developmental signals be used to regenerate projection neuron subtypes in the adult or in the dish? Here, we first provide an overview of the diversity and fate potential of neural progenitors of the cerebral cortex during development. Further, we discuss the plasticity of neural progenitors and the roles of intrinsic and extrinsic signals over progenitor fate. Finally, we discuss the relevance of developmental signals for efforts to direct the differentiation of pluripotent stem cells into specific types of cortical projection neurons for therapeutic benefit.

Indexed as

AnimalsCerebral CortexEmbryonic DevelopmentNerve RegenerationNeuronsPluripotent Stem Cells

Identifiers

PMID20681320
PMCPMC4226406

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.